Roles & Responsibilities :
- Minimum experience of 4 years in medical devices - Manufacturing Engineering.
- Good Experience working on Process Validations (IQ OQ PQ).
- Experience developing manufacturing processes and technologies which includes process characterization.
- Experience working on PFMEAs.
- Experience performing Data analysis (Minitab).
- Evaluate process and design alternatives based on Design for Manufacturability principles.
- Ability to work within a team and as an individual contributor in a fast-paced changing environment.
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
- Multitasks prioritizes and meets deadlines in timely manner.
- Strong organizational and follow-up skills as well as attention to detail.
- Complies with U.S. Food and Drug Administration (FDA) regulations other regulatory requirements Company policies operating procedures processes and task assignments.
Key Skills
Lean Manufacturing,Six Sigma,CNC Programming,Lean,Machining,Tooling,CAD,CNC,Assembly Experience,SolidWorks,Kaizen,Manufacturing
Employment Type : Full-time
Experience : years
Vacancy : 1